Phase
Condition
Anxiety Disorders
Panic Disorders
Stress
Treatment
Lion's mane and reishi blend
Lion's mane blend
Placebo
Clinical Study ID
Ages 18-26 All Genders Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Identify as a woman
Are aged 18 to 26 years at the time of giving consent (to be classified as Gen Zparticipants must have been born 1997-2013)
Rate themselves as stressed and/or anxious
Be a native speaker of English or fluent in English
Exclusion
Exclusion Criteria:
Have any pre-existing medical condition/illness which will impact taking part in thestudy. There may be other, unforeseen, exceptions and these will be considered on acase-by-case basis; i.e. participants may be allowed to progress to screening ifthey have a condition/illness which would not interact with the active treatments orimpede performance NOTE: the explicit exceptions to this is controlled hayfever,asthma, hypo/hyperthyroidism, high blood pressure, high cholesterol, reflux,dyslexia/dyscalculia, ADHD, autism.
Are currently taking prescription medications (NOTE: the explicit exceptions to thisare contraceptive treatments for female participants, and those taken 'as needed' inthe treatment of asthma and hay fever. There may be other instances of medicationuse which, where no interaction with the active treatments is likely, and whichwould not be expected to have any impact on brain function, participants may be ableto progress to screening). Within this trial medication for diagnosed neurologicalconditions (e.g. ADHD) will be allowed as long as medication has been taken for aminimum of 3 months and will be taken consistently throughout the trial period.
Have relevant food allergies/ intolerances/ sensitivities
Excessive caffeine intake (> 500 mg per day)
Have taken dietary supplements e.g. Vitamins, omega 3 fish oils etc. in the last 4weeks (Note: participation is possible following a 4 week supplement washout priorto participating and for the duration of the study on the proviso that thesupplements they are taken are out of choice and not medically prescribed oradvised. NOTE - Vitamin D and iron supplements are allowed for this trial if theyhave been advised by GP to increase levels to a normal range and have been taken forat least 4 weeks consistently and will be taken consistently throughout the trial.
Are pregnant, seeking to become pregnant or lactating
Have taken antibiotics within the past 4 weeks
Are currently participating in other clinical or nutrition intervention studies, orhave done so in the past 4 weeks
Has been diagnosed with/ undergoing treatment for alcohol or drug abuse in the last 12 months
Have been diagnosed with/ undergoing treatment for a psychiatric disorder in thelast 12 months (this includes medically diagnosed anxiety and depression)
Suffer from frequent migraines that require medication (more than or equal to 1 permonth)
Sleep disorders or are taking sleep aid medication
Have any known active infections
Will be non-compliant with treatment consumption
Study Design
Study Description
Connect with a study center
Brain, Performance and Nutrition Research Centre, Northumbria University
Newcastle upon Tyne, Tyne and Wear NE1 8ST
United KingdomSite Not Available

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